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6,7-dihydro-5H-2,2aλ4,3-trithia-cyclopenta[cd]indene | 37159-78-7

中文名称
——
中文别名
——
英文名称
6,7-dihydro-5H-2,2aλ4,3-trithia-cyclopenta[cd]indene
英文别名
5,6-dihydro-4H-benzo[1,2]dithiole-7-carbothioaldehyde;4,5-dihydro-3H-8lambda~4~-[1,2]dithiolo[4,5,1-hi][1,2]benzodithiole;3,4λ4,5-trithiatricyclo[5.3.1.04,11]undeca-1,4(11),6-triene
6,7-dihydro-5<i>H</i>-2,2aλ<sup>4</sup>,3-trithia-cyclopenta[<i>cd</i>]indene化学式
CAS
37159-78-7
化学式
C8H8S3
mdl
——
分子量
200.35
InChiKey
DEKIUUYPODQMNN-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

物化性质

  • 密度:
    1.71±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.2
  • 重原子数:
    11
  • 可旋转键数:
    0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.38
  • 拓扑面积:
    69.8
  • 氢给体数:
    0
  • 氢受体数:
    3

反应信息

  • 作为反应物:
    描述:
    6,7-dihydro-5H-2,2aλ4,3-trithia-cyclopenta[cd]indene 在 [NEt4][W(CO)5I] 、 silver nitrate 作用下, 以 二氯甲烷 为溶剂, 生成 alkaline earth salt of/the/ methylsulfuric acid
    参考文献:
    名称:
    Fluxional pentacarbonyltungsten(0)的硫醛的复合物和的1,6,6aλ硫酮化合价异构体4 -trithiapentalenes
    摘要:
    硝酸银与在1,6,6aλ存在四乙pentacarbonyliodotungstate(0)的反应4 - trithiapentalenes给出pentacarbonyltungsten的硫醛的(0)配合物和的1,6,6aλ硫酮化合价异构体4 -trithiapentalenes; 对称取代的络合物是通量的。
    DOI:
    10.1039/c39830000289
  • 作为产物:
    参考文献:
    名称:
    A New Synthetic Route to 3,4-Bridged 1,6,6aλ4-Trithiapentalenes
    摘要:
    研发了一种新的合成路线,用于3,4-桥联的1,6,6aλ4-三硫戊烯,基于环酮与Bredereck试剂的反应,然后用五硫磷或Lawesson试剂对酮类二烯胺进行硫化。
    DOI:
    10.1055/s-2001-15160
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文献信息

  • Dingwall,J.G. et al., Journal of the Chemical Society. Perkin transactions I, 1973, p. 2351 - 2358
    作者:Dingwall,J.G. et al.
    DOI:——
    日期:——
  • A New Synthetic Route to 3,4-Bridged 1,6,6aλ4-Trithiapentalenes
    作者:Wei Zhang、Yewande Henry
    DOI:10.1055/s-2001-15160
    日期:——
    A new synthetic route to 3,4-bridged 1,6,6aλ 4-trithiapentalenes is developed based on reactions of cyclic ketones with Bredereck's reagent followed by thiolation of keto dienamines with phosphorus pentasulfide or Lawesson's reagent.
    研发了一种新的合成路线,用于3,4-桥联的1,6,6aλ4-三硫戊烯,基于环酮与Bredereck试剂的反应,然后用五硫磷或Lawesson试剂对酮类二烯胺进行硫化。
  • Fluxional pentacarbonyltungsten(0) complexes of the thioaldehyde and thioketone valence isomers of 1,6,6aλ<sup>4</sup>-trithiapentalenes
    作者:Peter J. Pogorzelec、David H. Reid
    DOI:10.1039/c39830000289
    日期:——
    The reaction of silver nitrate with tetraethylammonium pentacarbonyliodotungstate(0) in the presence of 1,6,6aλ4- trithiapentalenes gives pentacarbonyltungsten(0) complexes of the thioaldehyde and thioketone valence isomers of 1,6,6aλ4-trithiapentalenes; the symmetrically substituted complexes are fluxional.
    硝酸银与在1,6,6aλ存在四乙pentacarbonyliodotungstate(0)的反应4 - trithiapentalenes给出pentacarbonyltungsten的硫醛的(0)配合物和的1,6,6aλ硫酮化合价异构体4 -trithiapentalenes; 对称取代的络合物是通量的。
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同类化合物

[1,2]二硫杂环戊烯并[1,5-b][1,2]二硫杂环戊烯 2,5-二苯基-6a-硫杂并噻吩 3-Brom-2,5-dimethyl-6a-thiathiophthen (1,2)Dithiolo(1,5-b)(1,2)dithiole-7-s(iv), 3,4-diphenyl- 1,4-Diisopropyl-6,7-dihydro-5H-2,2aλ4,3-trithia-cyclopenta[cd]indene 2,5-dimethyl-3,4-trimethylene-6a-thiathiophthene 2,5-Diethyl-3,4-trimethylen-6α-thia-thiophthen (1,2)Dithiolo(1,5-b)(1,2)dithiole-7-s(iv), 3,4-dimethyl- 2-Methylthio-5-phenyl-6a-thiathiophthen 2-Methyl-5-phenyl-6a-thiathiophthen 2,5-Dimethyl-3-[2-(2,2,2-trifluoro-1-trifluoromethyl-ethyl)-4-(2,2,2-trifluoro-1-trifluoromethyl-ethylidene)-[1,3]dithietan-2-yl]-7λ4-[1,2]dithiolo[1,5-b][1,2]dithiole 3-methyl-2,5-diphenyl-1,6,6aSIV-trithiapentalene 1-Phenyl-thiothiophthen 3,4-difluoro-2-mercapto-1,6,6aλ4-trithiapentalene 2-Phenyl-5--6α-thia-thiophthen 6,7-dihydro-5H-2,2aλ4,3-trithia-cyclopenta[cd]indene 2,4-diphenyl-1,6,6aλ4-trithiapentalene 2-methyl-1,6,6a-trithiapentalene 2,5-dimethyl-7λ4-[1,2]dithiolo[1,5-b][1,2]dithiole 2-Methyl-thiathiophthen 2-(4-Methylphenyl)-4,5,6,7-tetrahydro-9lambda~4~-[1,2]dithiolo[1,5-b][1,2]benzodithiole 2-Methyl-3,5-diphenyl-6α-thia-thiophthen 5-Phenyl-7λ4-[1,2]dithiolo[1,5-b][1,2]dithiole-2,3-dicarboxylic acid diethyl ester 2-(4,5-Dimethyl-7lambda~4~-[1,2]dithiolo[5,1-e][1,2]dithiol-2-yl)pyridine 2,5-Diphenyl-3,4-ethylen-1,6,6aλ4-trithiapentalen 1,6,6aIVS-Trithiapentalene, 3-phenyl- Dimethyl 5,6lambda4,7-trithiatricyclo[6.4.0.02,6]dodeca-1(8),2(6),3-triene-3,4-dicarboxylate 7,8lambda4,9-Trithiatetracyclo[6.6.0.02,6.010,14]tetradeca-1(8),2(6),10(14)-triene 2,5-Bis-methylthio-3,4-trimethylen-6aSIV-1,6,6a-trithia-pentalen